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Survey of Sand Flies (Diptera: Psychodidae) in an Environmentally Protected Area in Brazil

  • Lara Saraiva ,

    Contributed equally to this work with: Lara Saraiva, Célia Maria Ferreira Gontijo, José Dilermando Andrade Filho

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • Alanna Silva Reis ,

    ‡ These authors also contributed equally to this work.

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • Jeronimo Marteleto Nunes Rugani ,

    ‡ These authors also contributed equally to this work.

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • Agnes Antônia Sampaio Pereira ,

    ‡ These authors also contributed equally to this work.

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • Felipe Dutra Rêgo ,

    ‡ These authors also contributed equally to this work.

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • Ana Cristina Vianna Mariano da Rocha Lima ,

    ‡ These authors also contributed equally to this work.

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • Célia Maria Ferreira Gontijo ,

    Contributed equally to this work with: Lara Saraiva, Célia Maria Ferreira Gontijo, José Dilermando Andrade Filho

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

  • José Dilermando Andrade Filho

    Contributed equally to this work with: Lara Saraiva, Célia Maria Ferreira Gontijo, José Dilermando Andrade Filho

    Affiliation Grupo de Estudos em Leishmanioses–Centro de Pesquisas René Rachou–FIOCRUZ–MINAS–Avenida Augusto de Lima, 1715 Barro Preto, CP 1743, 30190–002 Belo Horizonte, MG, Brazil

Survey of Sand Flies (Diptera: Psychodidae) in an Environmentally Protected Area in Brazil

  • Lara Saraiva, 
  • Alanna Silva Reis, 
  • Jeronimo Marteleto Nunes Rugani, 
  • Agnes Antônia Sampaio Pereira, 
  • Felipe Dutra Rêgo, 
  • Ana Cristina Vianna Mariano da Rocha Lima, 
  • Célia Maria Ferreira Gontijo, 
  • José Dilermando Andrade Filho


Brazil is one of the most important endemic areas for leishmaniasis worldwide. Protected areas that are tourist attractions likely present an important risk of transmission of cutaneous leishmaniasis (CL). Furthermore, with the geographical expansion of visceral leishmaniasis (VL), several studies have recorded the occurrence of its vector, Lutzomyia longipalpis, and cases of human and canine VL in such tourist areas. The Parque Estadual do Sumidouro is an environmentally protected area located in the Brazilian Cerrado biome and in an important area endemic for leishmaniasis in the state of Minas Gerais. The purpose of this study was to monitor the sand fly fauna in areas of tourist activity in the park. Sampling was performed every month, from September 2011 to August 2013, using CDC light traps at six sites of differing environmental characteristics. Sampled specimens were identified following Galati (2003), and females were submitted to molecular techniques for the detection and identification of Leishmania DNA. A total of 4,675 sand fly specimens of 25 species belonging to nine genera were collected. The most abundant species were Micropygomyia quinquefer, Lutzomyia renei and Pintomyia pessoai, although only Pi. pessoai is implicated in the transmission of Leishmania braziliensis. The species accumulation curve reached saturation on the 16th sampling event. Species richness, diversity and evenness differed among the sampled areas. The seasonal curve was not determined by a single unique species, and no single species was the most abundant in all environments sampled. The main vector of Leishmania (Leishmania) infantum, Lutzomyia longipalpis, accounted for only 5.35% of the specimens collected. Proven or suspected vectors of Leishmania (Viannia) braziliensis were recorded, and one female of the cortellezzii complex tested positive for Le. braziliensis DNA. Even with a low infection rate (0.62%), these data indicate the circulation of the parasite and reinforce the need for entomological and epidemiological surveillance in the park and its surroundings.


Brazil is one of the most important areas of the world for the occurrence of endemic leishmaniasis. Given its high incidence and mortality rates in Brazil, much of the current attention has been given to urban foci of visceral leishmaniasis (VL). However, cutaneous leishmaniasis (CL) presents significant health problems in wild, rural and even urban and peri-urban areas [1] [2].

Environmentally protected areas that serve as tourist attractions may present an important CL transmission risk in southeastern Brazil. Typically, occupational exposure to CL transmission occurs when individuals are exposed to the focus of the disease, however, autochthonous cases have been recorded in urban and peri-urban areas [2]. With the geographical spread of VL, several studies have recorded populations of Lu. longipalpis and cases of human and canine VL in areas of more recent human settlement, including tourist areas [3] [4].

A survey of the protected area “Parque Estuadual do Alto Ribeira”, situated in a region endemic for CL, found the sand fly Nyssomyia intermedia (Lutz & Neiva, 1912), one of the main vectors of Le. braziliensis, to be the sixth most abundant sand fly species. This species had the highest rates of incidence in the camping area of the park where Lu. longipalpis was also recorded. Another study conducted in Bonito City, one of the main ecotourism destinations of Brazil, reported a high abundance of Lu. longipalpis as well as a high incidence of canine seroprevalence for Leishmania. Furthermore, Nyssomyia whitmani (Antunes & Coutinho, 1939), another main vector of Le. braziliensis, has been recorded in Bonito City. [5],[6].

The Parque Estadual do Sumidouro (Sumidouro State Park)–PES-, is situated in the Cerrado biome, known also as the Brazilian Savannah. The Cerrado is the second largest terrestrial biome in South America and occupies 22% of the land area of Brazil. Although the Cerrado is considered a global biodiversity hotspot, it is experiencing a remarkable amount of habitat destruction due to human occupation and activities such as urbanization and agricultural and coal production [7]. Such anthropogenic modifications can favor the occurrence of pathogens through the elimination of the natural habitats of reservoirs and vectors, thus causing the life cycles of these species to adapt to the modified environment [8], [9].

Knowledge of the risk of exposure to residents and tourists in these areas is essential for the surveillance and management of potential cases of leishmaniasis. Epidemiological data for areas frequently visited could be instrumental for the accurate diagnosis of leishmaniasis, and for the selection of treatment strategies, especially concerning tourists that return to non-endemic areas [10].

The purpose of the present study was to describe the sand fly fauna in PES, an area of protected Cerrado. The area is endemic for leishmaniasis, and has documented cases of both visceral and cutaneous human leishmaniasis. Located in PES is Lapinha’s cave, a taxonomically and biologically important site for the collection of Lutzomyia longipalpis [11] [12] [13] [14] [15].

Materials and Methods

Study area and collection of specimens

Sand flies were collected from six localities within PES of varying environmental characteristics, including type of vegetation, presence of rock formations, and degree of human disturbance. The PES is a thirteen-hundred hectare environmentally protected area located about 50 km from the city of Belo Horizonte, the capital of the state of Minas Gerais. The park is located in the Lagoa Santa karst region, with the relief being formed of carbonate rocks that are prone to dissolving with water [16] (Fig 1).

Fig 1. Map showing the location of PES and the location of sampling sites in the park.

(1)—Park surroundings—peridomestic areas; (2)—Cerrado 1; (3)—Cerrado 2; (4)—Rupicolous vegetation; (5)—Cave entrance; (6)—Cave surroundings.

The environment of each sampling site was briefly described considering characteristics that may favor the occurrence of sand flies. Environmental characteristics considered were those that related to:

  1. * Breeding, shelter and feeding on plants; presence and type of vegetation; presence of water collection sites; and the presence of rocks.
  2. * Haematophagic habit: presence of local fauna, including dogs.

The environmental characteristics of the collection sites are briefly described in Table 1. The area sampled was 0.08 km2, and the traps were arranged in a non-linear transect of 1000 meters. The selection of collection sites followed two criteria: (1) the sampling of all of the different environments of the park considering vegetation, topography and anthropogenic modification; (2) proximity to the trail most commonly used by tourists (the primary reason for the entomological surveillance program).

Table 1. Environmental characteristics of the sand fly collection sites in PES from September 2011 to August 2013.

Collection procedures were approved by the Ministério do Meio Ambiente do Brasil (Ministry of Environment of Brazil)—(SISBIO: 15,237 and 30297–2) and the Instituto Estadual de Florestas de Minas Gerais (State Forestry Institute of Minas Gerais) (072/11). Sampling took place over two years and was performed every month over three consecutive days using HP-model CDC light traps [17] arranged uniformly in the different study areas.

Twelve light traps were used: two traps were placed in the backyards of houses located in the park surroundings (peridomestic areas) and 10 traps were placed inside the park itself. Of the traps placed within the park, two were placed in forested/semi-deciduous forest (Cerrado 1), two in wooded/deciduous forest (Cerrado 2), two in rupicolous vegetation, two next to the entrance to the Lagoa do Sumidouro cave, and two in the area surrounding the cave.

The sampling transect was about 1000 meters in length (corresponding to a section of the main tourist trail of the park), with an average of 200 meters between trap sites. A total of only 0.08km2 (6.15%) of the entire 13,000 km2 of the park were sampled. Sampling took place from September 2011 to August 2013, with a total sampling effort of 20.736 hours.

Trapped specimens were identified according to the classification proposed by Galati (2003). Females belonging to the species Evandromyia sallesi (Galvão & Coutinho, 1940) and Evandromyia cortelezzii (Brethes, 1923), and belonging to the species Pintomyia mamedei (Oliveira, Afonso, Dias & Brazil, 1994) and Pintomyia christenseni (Young & Duncan, 1994), were identified as belonging to the cortelezzii complex and the mamedei complex, respectively, when morphological differentiation was inconclusive.

Female specimens collected up to April 2013 were processed for the detection of Leishmania DNA. These specimens were stored in DMSO 6% and frozen at -20°C. At the time of identification, the last three abdominal segments and the head of each female specimen were removed and mounted in Berlese liquid. Simultaneously, the gut was checked for the presence of blood. The remaining specimens were placed in 70% alcohol, prepared and mounted in Canada Balsam.

DNA extraction and polymerase chain reaction

DNA extraction employed the Puregene QIAGEN Gentra kit. The molecular target chosen for Leishmania DNA detection was the Internal Transcribed Spacer I (ITS I) of rDNA. [18]. The reaction protocol used was that established by Schonian et al 2003 [18] with some modifications. The positive controls were DNA of four reference strains: Leishmania braziliensis (MHOM/BR/75/M2903), Leishmania guyanensis (MHOM/BR/75/M4147), Leishmania infantum (MHOM/BR/74/PP75), and Leishamania amazonensis (IFLA/BR/67/PH8) at a concentration of 20 ng/μl. For species identification the amplified products were digested by the enzyme Hae III as described by Schonian et al 2003 [18].

If the restriction fragment analysis did not produce visible DNA bands, the whole fragment resulting from the PCR amplification of the ITS-1 region was sequenced. To purify the product QIAquick PCR Purification Kit (Qiagen) was used following the manufacturer’s instructions. Next, a mixture was prepared containing 1μL of purified products, 1μL of each primer at a concentration of 5 pmol, antisense or sense (in separate tubes), 1μL 5x Sequencing Buffer, 1μL of BigDye Terminator v3.1 Cycle Sequencing, and distilled water for a final volume of 10 μL. The program used 35 cycles alternating between 95°C for 15 seconds and 65°C for 15 seconds. The ITS-1 fragment sequences were read using an ABI 3730xl DNA Analyzer automatic DNA sequencer.

Data analysis

The focus of the present study was to perform a descriptive analysis of sand-fly population patterns in areas of Cerrado with different kinds of vegetation. Margalef diversity and J evenness indices were used for ecological analyses of the study areas since they are non-parametric indices, which are less influenced by differing sampling efforts. The Margalef diversity index is used to summarize information about the number of species and their abundance, and is employed to compare samples and locations. The J evenness index is used to describe the distribution of collected specimens among the species present, and thus is used to make inferences about species dominance in a population [19].

Descriptive analyses of all data were performed using Microsoft Excel (Office 2003). Graph Pad Prisma 4.0 software was used for statistical analyses and the PAST program was used for the ecological analyses. The entomological sampling sites were georeferenced using GPS—GARMIN eTrex-H for the spatial analysis of vector species (suspected and confirmed) population density. The coordinates and presence/absence data of vectors for each site were analyzed using ArcGIS 9.3 software.

For each study site, kernel estimation was used to infer vector density. This is a non-parametric statistical method of interpolation that identifies sites with the highest occurrence of a given event [20]. For kernel estimation in the present study, sand fly species were categorized as vectors (suspected or confirmed) or non-vectors of Leishmania species.

Sequences of the ITS-1 fragment were analyzed using Finch TV software (Geospiza, Inc.). Alignment of the sequences with sequences obtained from GenBank was performed using BLAST (


Sand fly fauna and environmental characteristics

A total of 4,675 sand fly specimens belonging to nine genera and 25 species were collected. The species with the highest abundance was Micropygomyia quinquefer (Dyar, 1929), which accounted for 37.54% of the total. The next most abundant species were Lutzomyia renei (Martins, Falcão & Silva, 1957) and Pintomyia pessoai (Barretto & Coutinho, 1940), with 22.67% and 9.52%, respectively (Table 2). Considering these three most abundant species, only Pi. pessoai is implicated in the transmission of Leishmania braziliensis. Species richness and diversity were relative high among the samplings (Tables 2 and 3, Fig 2). The species accumulation curve reached saturation at the 16th sampling event when the value stabilized at 25 species. The six sites had distinctly different values for the species richness, diversity, abundance, and equitability indices. Even in the small region of this protected area sampled, there is considerable heterogeneity in the sand fly composition among sampled sites (Tables 1 and 2).

Fig 2. Species accumulation curve, abundance, and species richness of the sand fly fauna of PES from September 2011 to August 2013.

Table 2. Species of sand flies collected by site in the PES, sex, and total percentage from September 2011 to August 2013.

Table 3. Diversity indices for the sand fly fauna of the collection sites in PES from September 2011 to August 2012.

The area referred to as Cerrado 1 (forested/semi-deciduous forest) had the highest values for the diversity index, followed by Cerrado 2 (wooded area/deciduous forest); both areas had high values of equitability. The localities with the lowest values for species richness were the Cave entrance and the Rupicolous area; both had the lowest values of equitability as well. These latter two environments, however, had the highest values for relative abundance (Table 2).

There is no single species that dominates all of the studied environments in the park. For instance, in the park surroundings, specimens of the cortelezzii complex and Evandromyia cortelezzii were the most predominantly collected, whereas in areas of Cerrado 1 (forested/semi-deciduous forest) and Cerrado 2 (wooded areas/deciduous forest) Pi. pessoai predominated. The most abundant species in the area of rupicolous vegetation and in the environment surrounding the cave was Mi. quinquerfer, and Lu. renei was the most common species in the cave entrance. The vector species Lu. longipalpis, Ny. intermedia and Ny. whitmani, were collected from all environments studied in the park. Migonemyia migonei (France, 1920) and Pintomyia fischeri (Pinto, 1926) were collected from five and four study areas, respectively.

During both years of sampling the most productive period of sand fly collection was from December to April, whereas the least productive was in June and July (Figs 2 and 3). The species with the highest abundance values, Mi. quinquefer and Lu. renei, did not determine the pattern of the seasonal curve (Fig 3). The analyses of the seasonal curve in relation to the climatic parameters showed peaks of sand fly abundance during warm and humid periods. Among the climatic parameters analyzed, only relative humidity was not statistically correlated with the seasonal curve [Temperature (p-value < 0,0001 – Spearman correlation test), Precipitation (p-value = 0,0013 – Spearman correlation test), Air relative humidity (p-value = 0,0984 – Spearman correlation test)].

Fig 3. Relationship between seasonal variation of sand fly abundance and the climate parameters of total precipitation, relative humidity and mean temperature in PES from September 2011 to July 2013.

The left Y-axis references the number of sandflies collected (total number) and the precipitation rate (mm3)—these data are represented by bars. The right Y-axis references the average temperature (°C) and relative air humidity (%)—these data are represented by lines with markers.

Leishmania DNA detection and identification

Of the total of 2,380 female specimens analyzed for the detection of Leishmania DNA, 1,014 were processed individually and 1,366 were grouped into 153 pools. These female sand flies were grouped according to species, collection date and collection site, with 2 to 20 individual sand flies in each pool (mean = 14). Only four individually processed samples tested positive for ITS-1 PCR (Table 4). The results of the RFLP reactions were not informative due to low DNA concentrations, and so the identification of samples was performed through the sequencing reaction. Only one sample was identified as Le. braziliensis and it was from a female of the cortelezzii complex. Two samples were identified as Crithidia fasciculata, one as a female Ev. sallesi and another as a female Psathyromyia lutziana (Costa Lima 1932). A female Sciopemyia sordellii (Shannon & Del Ponte, 1927) had a positive reaction for trypanosomatids. The natural infection rate of females of the cortelezzii complex by Le. braziliensis was 0.62%.

Table 4. Results of DNA detection and identification of species of Trypanosomatidae according to species of sand fly, collection sites, and collection date in PES from September 2011 to August 2013.

Vectors density analyses

The map of suspected or proven vector species shows that they were distributed among all of the collection sites in PES, with the highest concentration of vector species occurring at the cave entrance and the areas of forested/semi-deciduous forest and wooded/deciduous forest. The area of rupicolous vegetation had intermediate vector densities, whereas the peridomestic localities surrounding the park had the lowest vector densities (Fig 4).


The PES is located in the municipalities of Lagoa Santa and Pedro Leopoldo, both of which have historical records of human cases of VL and CL and report cases of canine leishmaniasis. From 2009 to 2013, three cases of VL were documented in Lagoa Santa and two in Pedro Leopoldo. During the same time period, three cases of CL were reported in Lagoa Santa and six in Pedro Leopoldo [21].

Among the proven or suspected vector species collected in the park, Lu. longipalpis accounted for 5.35%. Although this species was collected in all of the environments sampled, it was most abundant at the cave entrance. This species was also collected in high numbers in less anthropogenetically influenced habitats, with only one specimen being collected in the peridomestic environment.

The data of this study are consistent with the hypothesis that different populations of Lu. longipalpis have different behavior patterns in different environments. However, it may be that this species merely possesses an enormous ability to adapt to anthropogenically modified environments [22], [23], [24], [25].

A large number of species that are suspected or proven vectors of Le. braziliensis were documented in PES, such as Ny. whitmani [26]. Moreover, Le. infantum DNA was detected in females of Ny.whitmani in different areas of Minas Gerais State [27], [28]. This species has a tendency to adapt to anthropogenically influenced areas in spite of its greatest abundances in natural areas and forest environments [29], [30], [31].

Specimens of Ev. sallesi and Ev. cortelezzii, as well as specimens of the cortelezzii complex, are suspected of participating in the transmission cycles of Leishmania sp. These species are frequently collected in peridomestic environments, and the DNA of Le. infantum has been detected in both Ev. sallesi and Ev. cortelezzii. Furthermore, specimens of the cortelezzii complex have been found positive for Le. braziliensis DNA [28], [32]. In southeastern Brazil, Ny. intermedia, Nyssomyia neivai (Pinto, 1926), Mi. migonei, Pi. pessoai and Pi. fischeri have been incriminated in the transmission of Le. braziliensis, [28], [29], [33], [34], [35], [36], [37], [38].

Species whose participation in the transmission cycles of leishmaniasis need to be further clarified were also collected, such as Evandromyia lenti (Mangabeira 1938) and Sc. sordellii [27], [39], [40], [41]. The remaining species of sand flies recorded in PES are not suspected to be involved in the transmission cycles of Leishmania spp.

So far the indices of species richness, diversity and abundance recorded among the park localities have been described through simple descriptive analysis. Additional analyses using non-parametric statistical methods provide a similar interpretation [19], [42].

In every sampling, the study areas that had elevated values of diversity remained relatively stable throughout the study period, which agrees with what is expected of an environmentally preserved area (Tables 1 and 2). In PES evenness was high and there was not a single species that represented more than 40% of the sand fly specimens collected in the park (Table 1). These data agree with other studies in which natural areas tended to have greater species richness and diversity. For example, a study conducted on Ilha Grande, RJ, Brazil, a recent transmission area of Le. infantum, higher species richness and abundance were found in areas with lower anthropogenic modification [38].

In a study in the state of Espírito Santo, Brazil, a similar pattern was found in tropical forest areas and the authors emphasize that conserved areas have greater opportunities for shelter and more sources of food for sand flies [43]. These data concur with classical ecological theories that postulate that the greater diversity of habitats favors the greater biodiversity of species [44].

The present data analysis shows that the environmental diversity of the park holds highly differentiated faunistic compositions even in proximate sampling sites. For instance, the species of the genus Brumptomyia [(Brumptomyia brumpt (Larrousse, 1920) and Brumptomyia avellari (Costa Lima, 1932)] were not recorded from the peridomestic environments and had higher relative abundances in Cerrado 1 and Cerrado 2. This pattern of occurrence is consistent with other faunal surveys [31], [45], [46]. Similar distribution patterns were also observed for other species (Table 1).

Although sand flies have not traditionally been considered in ecological conservation studies, the data herein corroborates and reinforces studies that call for better strategies to protect the Brazilian Cerrado biome [47]. Given the ecological complexity of the sand fly fauna of PES, it could be inferred that other invertebrate groups of the region, that have not yet been investigated, could be under risk due to impacts to the entire biome. These findings in PES agree with general descriptions of the Cerrado biome; the environmental diversity of Brazilian Cerrado forms a complex mosaic of habitats with different vegetation types, which contributes to a non-uniform species distribution [7].

The biodiversity of the park area is clearly demonstrated by the seasonal curve, which is influenced by several species. For example, My. quinquerfer and Lu. renei are responsible for the highest peaks of sand fly occurrence in the park, however, their individual patterns differ. The pattern of the seasonal curve in PES is in accordance with other studies carried out in the city of Belo Horizonte and in the region of Lapinha’s cave [11], [30]. However, these results differ from others studies conducted in Belo Horizonte in which peaks in warmer and rainy months are not so evident [48]. These results demonstrate that entomological monitoring is required for leishmaniasis prevention and control measures based on vector control strategies because seasonal patterns of variation are prone to change due to environmental factors and insect community composition.

Only one female of the cortelezzi complex was found to be positive for Le. braziliensis DNA. Even if representing a low infection rate (0.62%), this observation indicates the circulation of the parasite in the area and reinforces the need for entomological and epidemiological surveillance. It is important to note that the molecular marker used in this study, the ITS-1 region, was specifically designated for detecting the genus Leishmania [49], however, in this work the region was able to detect another genus of the family Tripanosomatidae; two females tested positive for the genus Chritidia.

The vector distribution map summarizes the distribution of epidemiological risk since it shows significant vector density. As reported in other studies, the risk is not equally distributed among sampling localities; there is a higher record of vector species, or potential vectors, in locations with certain environmental characteristics [30], [50], [51]. Modern public health practices now possess the tools necessary to analyze key points in the relationship between the events involved in human diseases [52], [53].

These results underscore the need for entomological vigilance in PES where the presence of vectors, and the proximity of important endemic areas, suggest the possible establishment of cycles involving the parasites. A total of 14 sand fly species with proven or suspected involvement in the transmission cycles of Le. infantum and Le. braziliensis in Brazil were recorded in PES. The main vector species of Le. infantum, Lu. longipalpis, was detected in this study, whereas 13 species related to the transmission cycles of Le. braziliensis were recorded. Furthermore, the tourist potential of the park and, the tendency for an increasing number of visitors, reinforce the need to establish entomological monitoring in the area. This type of situation has been described in other tourist areas in Brazil [38], [54].

It is not possible to ignore human factors in considering control measures of endemic diseases and improvements are needed in the way of entomological monitoring in order to employ preventive actions. This need is reinforced by the increasing amount of tourism in the area [55].


Our data show the presence of confirmed and suspected vector species of Leishmania infatum and Leishmania braziliensis at all sampling points along the main tourist trail in PES. This, along with the finding of Le. braziliensis in one female of the cortellezzi complex, demonstrate the need for continuing entomological and epidemiological surveillance in PES.


The authors are grateful to the community of the Parque Estadual do Sumidouro for their collaboration in the field sampling process.

Author Contributions

Conceived and designed the experiments: JDAF CMFG LS. Performed the experiments: JDAF CMFG LS ASR FDR JMNR AASP ACVMRL. Analyzed the data: JDAF CMFG LS FDR. Contributed reagents/materials/analysis tools: JDAF CMFG LS. Wrote the paper: JDAF CMFG LS.


  1. 1. Brasil Ministério da Saúde. Manual de Vigilância e Controle da Leishmaniose Visceral. 2006. p. 122.
  2. 2. Ministério B, Vigilância S De. Manual de Vigilância da Leishmaniose Tegumentar Americana. 2010.
  3. 3. Souza CF, Borges M a Z, Andrade AJ. Contribution to the knowledge of the phlebotomine sand flies fauna (Diptera: psychodidae) of Timóteo municipality, Minas Gerais, Brazil. Neotrop Entomol. 2009;38: 267–71. Available: pmid:19488518
  4. 4. State SP, Galati EAB, Marassá AM, Gonçalves-andrade RM, Consales CA, Fátima E, et al. Phlebotomines (Diptera, Psychodidae) in the Speleological Province of the Ribeira Valley : 2. Parque Estadual do Alto Ribeira. 2010;477: 477–487.
  5. 5. Aparecida E, Galati B, Marassá AM, Gonçalves-andrade RM, Consales CA, Bueno EFM. Phlebotomines (Diptera, Psychodidae) in the Ribeira Valley Speleological Province – 1. Parque Estadual Intervales, state of São Paulo, Brazil. 2010;54: 311–321.
  6. 6. Mato E De, Rachel A, Andrade O De, Lúcia V, Nunes B, Aparecida E, et al. Epidemiological study on leishmaniasis in an area of environmental tourism and ecotourism, State of Mato Grosso do Sul, 2006–2007 Estudo epidemiológico das leishmanioses em área de turismo ambiental e. 2009;42: 488–493.
  7. 7. Ministério do Meio Ambiente—Brazil [Internet]. 2014 p. 2014. Available:>
  8. 8. Gomes A de C, Neves VLF de C. Estratégia e perspectivas de controle da leishmaniose tegumentar no Estado de São Paulo The strategy and prospects for the control of cutaneous leishmaniasis in the State of São Paulo. Rev Soc Bras Med Trop. 1998;31: 553–558. pmid:9859700
  9. 9. Correa Antonialli SA, Torres TG, Paranhos Filho AC, Tolezano JE. Spatial analysis of American Visceral Leishmaniasis in Mato Grosso do Sul State, Central Brazil. J Infect. 2007;54: 509–14. pmid:16979241
  10. 10. Scarisbrick JJ, Chiodini PL, Watson J, Moody a, Armstrong M, Lockwood D, et al. Clinical features and diagnosis of 42 travellers with cutaneous leishmaniasis. Travel Med Infect Dis. 2006;4: 14–21. pmid:16887720
  11. 11. Andrade Filho, J. D., Lima M. L. N., Falcão A. L., Brazil RP. Sazonalidade dos flebotomíneos dos arredores da Gruta da Lapinha, município de Lagoa Santa, Minas Gerais. Rev Bras Entomol. 1998;42: 93–95.
  12. 12. Hooper a. M, Farcet J-B, Mulholland NP, Pickett J a. Synthesis of 9-methylgermacrene B, racemate of the sex pheromone of Lutzomyia longipalpis (Lapinha), from the renewable resource, Geranium macrorrhizum essential oil. Green Chem. 2006;8: 513.
  13. 13. Yin H, Mutebi JP,Marriott S,Lanzaro GC—Metaphase karyotypes and G-banding in sandflies of the Lutzomyia longipalpis complex. Med Vet Entomol. 1999 Feb;13(1):72–7. pmid:10194752
  14. 14. Muto S, Nishimura Y, Mori K. Pheromone Synthesis, CXCVI [Synthesis of Germacrene-B and Its Extension to the Synthesis of (؎) -9-Methylgermacrene-B, the Racemate of the Male-Produced Sex Pheromone of the Sandfly Lutzomyia longipalpis from Lapinha, Brazil. 1999. Eur. J.Org. Chem., 2159–2165
  15. 15. Cardim MF, Rodas LA, Dibo MR, Guirado MM, Oliveira AM, Chiaravalloti-Neto F. Introduction and expansion of human American visceral leishmaniasis in the state of Sao Paulo, Brazil, 1999–2011. Rev Saude Publica. 2013;47: 691–700. pmid:24346660
  16. 16. Instituto Estadual de Florestas–[Internet]. 2013 p. 2013. Available:
  17. 17. Pugedo H, Barata RA, Franca-Silva JC, Silva JC, Dias ES. [HP: an improved model of suction light trap for the capture of small insects]. Rev Soc Bras Med Trop. 2005;38: 70–72. /S0037-86822005000100017 pmid:15717102
  18. 18. Schönian G, Nasereddin A, Dinse N, Schweynoch C, Schallig HDF., Presber W, et al. PCR diagnosis and characterization of Leishmania in local and imported clinical samples. Diagn Microbiol Infect Dis. 2003;47: 349–358. pmid:12967749
  19. 19. Magurran AE. Measuring Biological Diversity. 2004- Blackwell Publishing Company. 2004. pp. 285–286.
  20. 20. Saúde M da. Introduçao à Estatistíca Espacial para Saúde Pública. Capacitaçao e atualizaçao em geoprocessamento em saúde. 2007. p. 124. Available:
  21. 21. Sistema Nacional de Agravos de Notificação [Internet]. 2014. Available:
  22. 22. Bauzer LG, Souza NA, Ward RD, Kyriacou CP, Peixoto AA. The period gene and genetic differentiation between three Brazilian populations of Lutzomyia longipalpis. Insect Mol Biol. 2002;11: 315–323. Available: pmid:12144696
  23. 23. Bauzer LG, Gesto JS, Souza NA, Ward RD, Hamilton JG, Kyriacou CP, et al. Molecular divergence in the period gene between two putative sympatric species of the Lutzomyia longipalpis complex. Mol Biol Evol. 2002;19: 1624–1627. Available: pmid:12200489
  24. 24. Bottecchia M, Oliveira SG, Bauzer LG, Souza NA, Ward RD, Garner KJ, et al. Genetic divergence in the cacophony IVS6 intron among five Brazilian populations of Lutzomyia longipalpis. J Mol Evol. 2004;58: 754–761. pmid:15461432
  25. 25. Souza N a, Andrade-Coelho C a, Vigoder FM, Ward RD, Peixoto A a. Reproductive isolation between sympatric and allopatric Brazilian populations of Lutzomyia longipalpis s.l. (Diptera: Psychodidae). Mem Inst Oswaldo Cruz. 2008;103: 216–9. Available: pmid:18425278
  26. 26. Lainson R, Rangel EF. Lutzomyia longipalpis and the eco-epidemiology of American visceral leishmaniasis, with particular reference to Brazil: a review. Mem Inst Oswaldo Cruz. 2005;100: 811–827. /S0074-02762005000800001 pmid:16444411
  27. 27. Margonari C, Soares RP, Andrade-Filho JD, Xavier DC, Saraiva L, Fonseca AL, et al. Phlebotomine sand flies (Diptera: Psychodidae) and Leishmania infection in Gafanhoto Park, Divinopolis, Brazil. J Med Entomol. 2010;47: 1212–1219. Available: pmid:21175074
  28. 28. Saraiva L, Andrade Filho JD, Silva Sde O, Andrade AS, Melo MN. The molecular detection of different Leishmania species within sand flies from a cutaneous and visceral leishmaniasis sympatric area in Southeastern Brazil. Mem Inst Oswaldo Cruz. 2010;105: 1033–1039. Available: pmid:21225201
  29. 29. Carvalho GML, Gontijo CMF, Falcão AL, Andrade Filho JD. Study of Phlebotomine Sand Flies (Diptera: Psychodidae) Collected in a Leishmania-Endemic Area of the Metropolitan Region of Belo Horizonte, Brazil. J Med Entomol. 2010;47: 972–976. pmid:21175043
  30. 30. Saraiva L, Andrade Filho JD, Falcão AL, de Carvalho DAA, de Souza CM, Freitas CR, et al. Phlebotominae fauna (Diptera: Psychodidae) in an urban district of Belo Horizonte, Brazil, endemic for visceral leishmaniasis: Characterization of favored locations as determined by spatial analysis. Acta Trop. 2011;117: 137–145. pmid:21110938
  31. 31. Nascimento BW, Saraiva L, Neto RG, Meira PC, Sanguinette Cde C, Tonelli GB, et al. Study of sand flies (Diptera: Psychodidae) in visceral and cutaneous leishmaniasis areas in the central-western state of Minas Gerais, Brazil. Acta Trop. 2013;125: 262–268. pmid:23178219
  32. 32. Carvalho GML, Andrade Filho JD, Falcao AL, Rocha Lima ACVM, Gontijo CMF. Naturally infected Lutzomyia sand flies in a Leishmania-endemic area of Brazil. Vector Borne Zoonotic Dis. 2008;8: 407–414. pmid:18429695
  33. 33. Foratini OP. Entomologia Médica. São Paulo, E. Blücher/ EDUSP; 1973. p. 658.
  34. 34. Rangel EF, de Souza NA, Wermelinger ED, Barbosa AF. [Natural infection of Lutzomyia intermedia Lutz & Neiva, 1912, in an endemic area of visceral leishmaniasis of Rio de Janeiro]. Mem Inst Oswaldo Cruz. 1984;79: 395–396. Available: pmid:6535924
  35. 35. Andrade Filho JD, Galati EAB, Falcão AL. Nyssomyia intermedia (Lutz & Neiva, 1912) and Nyssomyia neivai (Pinto, 1926) (Diptera: Psychodidae: Phlebotominae) geographical distribution and epidemiological importance. Mem Inst Oswaldo Cruz. 2007;102: 481–487. pmid:17612769
  36. 36. Aguiar GM, de Azevedo AC, Medeiros WM, Alves JR, Rendeiro V. Aspects of the ecology of phlebotomines (Diptera: Psychodidae: Phlebotominae) in an area of cutaneous leishmaniasis occurrence, municipality of Angra dos Reis, coast of Rio de Janeiro State, Brazil. Rev Inst Med Trop Sao Paulo. 2014;56: 143–149. pmid:24626417
  37. 37. Teodoro U, Salvia Filho VL, de Lima EM, Spinosa RP, Barbosa OC, Ferreira ME, et al. [Phlebotomines in an area of transmission of tegumentar leishmaniasis in the northern region of Parana State, Brazil: seasonal variation and nocturnal activity]. Rev Saude Publica. 1993;27: 190–194. Available: pmid:8115833
  38. 38. Carvalho BM, Maximo M, Costa WA, de Santana ALF, da Costa SM, da Costa Rego TAN, et al. Leishmaniasis transmission in an ecotourism area: potential vectors in Ilha Grande, Rio de Janeiro State, Brazil. Parasit Vectors. 2013;6: 325. pmid:24499568
  39. 39. Brazil RP, Carneiro VL, Andrade Filho JD, Alves JCM, Falcão AL. Biology of Lutzomyia lenti (Mangabeira) (Diptera: Psychodidae). Anais da Sociedade Entomológica do Brasil. 1997. pp. 191–193.
  40. 40. Sherlock IA, Maia H, Dias-Lima AG. [Preliminary results of a project about the ecology of Phlebotomus vectors of cutaneous leishmaniasis in the state of Bahia]. Rev Soc Bras Med Trop. 1996;29: 207–214. Available: pmid:8713612
  41. 41. Carvalho GM, Brazil RP, Ramos MC, Serra e Meira PC, Zenobio AP, Botelho HA, et al. Ecological aspects of phlebotomine sandflies (Diptera: Psychodidae) from a cave of the speleological province of Bambui, Brazil. PLoS One. 2013;8: e77158. pmid:24130847
  42. 42. Barrantes G, Sandoval L. Conceptual and statistical problems associated with the use of diversity indices in ecology. Rev Biol Trop. 2009;57: 451–460. Available: pmid:19928446
  43. 43. Pinto Ide S, Ferreira AL, Valim V, Carvalho Fdos S, da Silva GM, Falcao AL, et al. Sand fly vectors (Diptera, Psychodidae) of American visceral leishmaniasis areas in the Atlantic Forest, State of Espirito Santo, southeastern Brazil. J Vector Ecol. 2012;37: 90–96. pmid:22548541
  44. 44. MEATYARD B. Ecology–From Individuals to Ecosystems, 4th ed., Michael Begon, Colin R. Townsend , John L. Harper, Blackwell Publishing, Oxford, 2005, 738 pages, Price £37.50 (paperback) ISBN: 1405111178. Biological Conservation. 2007. pp. 309–309.
  45. 45. Saraiva L, Lopes J dos S, Oliveira GBM, Batista F de A, Falcão AL, Andrade Filho JD. Estudo dos flebotomíneos (Diptera: Psychodidae) em área de leishmaniose tegumentar americana nos municípios de Alto Caparaó e Caparaó, Estado de Minas Gerais. Revista da Sociedade Brasileira de Medicina Tropical. 2006. pp. 56–63.
  46. 46. Perez J, Virgen A, Rojas JC, Rebollar-Tellez EA, Alfredo C, Infante F, et al. Species composition and seasonal abundance of sandflies (Diptera: Psychodidae: Phlebotominae) in coffee agroecosystems. Mem Inst Oswaldo Cruz. 2014;109: 80–86. pmid:24271002
  47. 47. WWF–Brasil 2014 – Cerrado [Internet]. 2014 p. 2014. Available:
  48. 48. Souza CM De, Pessanha JE, Barata RA, Monteiro EM, Costa DC, Dias ES. Study on phlebotomine sand fly (Diptera: Psychodidae) fauna in Belo Horizonte, state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz. 2004;99: 795–803. /S0074-02762004000800003 pmid:15761593
  49. 49. Dweik A, Schonian G, Mosleh IM, Karanis P. Evaluation of PCR-RFLP (based on ITS-1 and HaeIII) for the detection of Leishmania species, using Greek canine isolates and Jordanian clinical material. Ann Trop Med Parasitol. 2007;101: 399–407. pmid:17550645
  50. 50. Margonari C, Freitas CR, Ribeiro RC, Moura AC, Timbo M, Gripp AH, et al. Epidemiology of visceral leishmaniasis through spatial analysis, in Belo Horizonte municipality, state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz. 2006;101: 31–38. /S0074-02762006000100007 pmid:16699707
  51. 51. Machado da Silva AV, Magalhães MDAFM, Peçanha Brazil R, Carreira JCA. Ecological study and risk mapping of leishmaniasis in an endemic area of Brazil based on a geographical information systems approach. Geospat Health. 2011;6: 33–40. Available: pmid:22109861
  52. 52. Rushton G. Public health, GIS, and spatial analytic tools. Annu Rev Public Heal. 2003;24: 43–56.
  53. 53. Brasil Ministério da Saúde. Introduçao à Estatistíca Espacial para Saúde Pública. Brasília—DF; 2007. p. 124.
  54. 54. De Souza CF, Quaresma PF, Andrade Filho JD, Bevilacqua PD. Phlebotomine fauna in the urban area of Timoteo, State of Minas Gerais, Brazil. Acta Trop. 2014;134: 72–79. pmid:24613154
  55. 55. Gomes A de C. Vigilância Entomológica. Informe Epidemiológico do SUS. 2002 11: 79–90.